Canonical Allele Identifier: CA2639237431

Gene: ACE

Linked Data

• gnomAD v4: 17-63477608-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477613dup , CM000679.2:g.63477613dup	GRCh38
NC_000017.10:g.61554974dup , CM000679.1:g.61554974dup	GRCh37
NC_000017.9:g.58908706dup	NCBI36
NG_011648.1:g.5541dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.249+270dup MANE Select	ENSP00000290866.4:n.249+270dup
ENST00000290866.9:c.249+270dup	ENSP00000290866.4:n.249+270dup
ENST00000428043.5:c.249+270dup	ENSP00000397593.2:n.249+270dup
ENST00000579462.1:n.274+270dup
ENST00000580318.1:n.121dup
ENST00000582627.1:c.72dup	ENSP00000462280.1:p.Ala25ArgfsTer?
ENST00000582678.5:c.249+270dup	ENSP00000462995.1:n.249+270dup
ENST00000583336.5:n.283+270dup
ENST00000584529.5:n.283+270dup
NM_000789.3:c.249+270dup	NP_000780.1:n.249+270dup
XM_005257110.1:c.-207+270dup	XP_005257167.1:n.-207+270dup
NM_000789.4:c.249+270dup MANE Select	NP_000780.1:n.249+270dup
NM_001382700.1:c.14+270dup	NP_001369629.1:n.14+270dup
NM_001382701.1:c.-366+270dup	NP_001369630.1:n.-366+270dup